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pro vyhledávání: '"elevated ethylmalonic acid"'
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Ethylmalonic encephalopathy (EE) is a very rare autosomal recessive metabolic disorder that primarily affects children. Less than one hundred EE patients have been diagnosed worldwide. The clinical manifestations include chronic diarrhea, petechiae,
Externí odkaz:
https://doaj.org/article/e3bc108f036240b6b8857c0e50d78451
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Ethylmalonic encephalopathy (EE) is a very rare autosomal recessive metabolic disorder that primarily affects children. Less than one hundred EE patients have been diagnosed worldwide. The clinical manifestations include chronic diarrhea, petechiae,
Publikováno v:
Frontiers in Genetics
Ethylmalonic encephalopathy (EE) is a very rare autosomal recessive metabolic disorder that primarily affects children. Less than one hundred EE patients have been diagnosed worldwide. The clinical manifestations include chronic diarrhea, petechiae,
Akademický článek
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